rs1567721991, PRMT7

N. diseases: 9
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Intrauterine retardation
CUI: C1386048
Disease: Intrauterine retardation
0.700 CausalMutation CLINVAR
Global developmental delay
CUI: C0557874
Disease: Global developmental delay
0.700 CausalMutation CLINVAR
Infantile sensorineural hearing impairment
CUI: C4021535
Disease: Infantile sensorineural hearing impairment
0.700 CausalMutation CLINVAR
SHORT STATURE, BRACHYDACTYLY, INTELLECTUAL DEVELOPMENTAL DISABILITY, AND SEIZURES
CUI: C4310689
Disease: SHORT STATURE, BRACHYDACTYLY, INTELLECTUAL DEVELOPMENTAL DISABILITY, AND SEIZURES
0.700 CausalMutation CLINVAR
Preauricular skin tag
CUI: C1860816
Disease: Preauricular skin tag
0.700 CausalMutation CLINVAR
Sunken eyes
CUI: C0423224
Disease: Sunken eyes
0.700 CausalMutation CLINVAR
Polyhydramnios
CUI: C0020224
Disease: Polyhydramnios
0.700 CausalMutation CLINVAR
Infantile axial hypotonia
CUI: C3806604
Disease: Infantile axial hypotonia
0.700 CausalMutation CLINVAR
Brachydactyly
CUI: C0221357
Disease: Brachydactyly
0.700 CausalMutation CLINVAR